Canonical Allele Identifier: CA1374121579
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266818_72266820delinsCAA , CM000665.2:g.72266818_72266820delinsCAA GRCh38
NC_000003.11:g.72315969_72315971delinsCAA , CM000665.1:g.72315969_72315971delinsCAA GRCh37
NC_000003.10:g.72398659_72398661delinsCAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8288_835+8290delinsTTG